deltatrials
Completed PHASE3 INTERVENTIONAL 3-arm NCT03872232

Evaluating the Efficacy and Safety of Co-administrated Rosuvastatin/Ezetimibe and Telmisartan

A Randomized, Double-blind, Active-controlled, Multicenter Phase3 Trial to Evaluate the Efficacy and Safety of Co-administrated Rosuvastatin/Ezetimibe and Telmisartan in Patients With Primary Hypercholesterolemia and Essential Hypertension

Sponsor: Addpharma Inc.

Updated 6 times since 2019 Last updated: Jan 13, 2021 Started: Feb 26, 2019 Primary completion: Aug 12, 2020 Completion: Aug 12, 2020
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE3 trial investigates Hypercholesterolemia and Hypertension and is currently completed. Addpharma Inc. leads this study, which shows 6 recorded versions since 2019 — indicating limited longitudinal coverage. Heart and vascular conditions benefit from the kind of long-term tracking this trial provides.

Status Flow

~Apr 2019 – ~Jan 2021 · 21 months · monthly snapshotActive Not Recruiting~Jan 2021 – ~Feb 2021 · 31 days · monthly snapshotActive Not Recruiting~Feb 2021 – ~Jul 2024 · 41 months · monthly snapshotCompleted~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotCompleted~Sep 2024 – ~Sep 2025 · 12 months · monthly snapshotCompleted~Sep 2025 – present · 10 months · monthly snapshotCompleted

Change History

6 versions recorded
  1. Sep 2025 — Present [monthly]

    Completed PHASE3

  2. Sep 2024 — Sep 2025 [monthly]

    Completed PHASE3

  3. Jul 2024 — Sep 2024 [monthly]

    Completed PHASE3

  4. Feb 2021 — Jul 2024 [monthly]

    Completed PHASE3

    Status: Active Not RecruitingCompleted

  5. Jan 2021 — Feb 2021 [monthly]

    Active Not Recruiting PHASE3

Show 1 earlier version
  1. Apr 2019 — Jan 2021 [monthly]

    Active Not Recruiting PHASE3

    First recorded

Feb 2019

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Addpharma Inc.
Data source: Addpharma Inc.

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations